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Fragmentation pathways for selected electronic states of the acetylene dication

T Osipov et al 2008 J. Phys. B: At. Mol. Opt. Phys. 41 091001 (5pp)   doi: 10.1088/0953-4075/41/9/091001  Help

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T Osipov1, T N Rescigno1, T Weber1, S Miyabe2, T Jahnke3, A S Alnaser4,5, M P Hertlein1, O Jagutzki3, L Ph H Schmidt3, M Schöffler3, L Foucar3, S Schössler3, T Havermeier3, M Odenweller3, S Voss3, B Feinberg1, A L Landers6, M H Prior1, R Dörner3, C L Cocke4 and A Belkacem1
1 Lawrence Berkeley National Laboratory, Chemical Sciences, Berkeley, CA 94720, USA
2 Department of Chemistry, University of California, Davis, CA 9566, USA
3 Institut für Kernphysik, J W Goethe-Universität Frankfurt am Main, Max-von-Laue-Str. 1, D-60438 Frankfurt, Germany
4 Department of Physics, Kansas State University, Manhattan, KS 66506, USA
5 Physics Department, American University of Sharjah, Sharjah, UAE
6 Department of Physics, Auburn University, AL 36849, USA
E-mail: TYOsipov@lbl.gov

Abstract. Coincident measurement of the Auger electron and fragment ion momenta emitted after carbon core-level photoionization of acetylene has yielded new understanding of how the dication fragments. Ab initio calculations and experimental data, including body-frame Auger angular distributions, are used to identify the parent electronic states and together yield a comprehensive map of the dissociation pathways which include surface crossings and barriers to direct dissociation. The Auger angular distributions for certain breakup channels show evidence of core–hole localization.

Print publication: Issue 9 (14 May 2008)
Received 24 March 2008, in final form 25 March 2008
Published 23 April 2008

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